| Product NDC: | 17856-0608 |
| Proprietary Name: | Promethazine Hydrochloride |
| Non Proprietary Name: | Promethazine Hydrochloride |
| Active Ingredient(s): | 6.25 mg/5mL & nbsp; Promethazine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17856-0608 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087953 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19821115 |
| Package NDC: | 17856-0608-5 |
| Package Description: | 5 mL in 1 CUP (17856-0608-5) |
| NDC Code | 17856-0608-5 |
| Proprietary Name | Promethazine Hydrochloride |
| Package Description | 5 mL in 1 CUP (17856-0608-5) |
| Product NDC | 17856-0608 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazine Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19821115 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 6.25 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |